RecallHawk

Anker PowerCore 10000 power banks (model A1263 only)

Anker Innovations Limited, of China

Summary

CPSC recall: Anker PowerCore 10000 power banks (model A1263 only). By Anker Innovations Limited, of China. Hazard: The lithium-ion battery in the power bank can overheat, posing fire and burn hazards to consumers.. Remedy: Consumers should immediately stop using the recalled power banks and contact Anker Innovations for instructions on receiving a free replacement power bank. Visit https://www.anker.com/product-recalls to register for the recall. To receive a replacement, consumers will be requi

Details

Source

CPSC Consumer Product Recall

External ID

10311

Action Date

2025-06-12

Status

Recalled

Category

consumer_product

Product Description

This recall involves Anker PowerCore 10000 power banks with model number A1263. The brand name "Anker" is engraved on th

Context & Analysis

This is a unclassified recall.

This was one of 22 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Anker Innovations Limited, of China has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Anker Innovations Limited, of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Anker Innovations Limited, of China have FDA actions?

Anker Innovations Limited, of China has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10311" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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